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细胞因子释放综合征与癌症免疫疗法——历史挑战与光明前景。

Cytokine release syndrome and cancer immunotherapies - historical challenges and promising futures.

机构信息

In vivo Services, The Jackson Laboratory, Sacramento, CA, United States.

Technical Information Services, The Jackson Laboratory, Bar Harbor, ME, United States.

出版信息

Front Immunol. 2023 May 25;14:1190379. doi: 10.3389/fimmu.2023.1190379. eCollection 2023.


DOI:10.3389/fimmu.2023.1190379
PMID:37304291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10248525/
Abstract

Cancer is the leading cause of death worldwide. Cancer immunotherapy involves reinvigorating the patient's own immune system to fight against cancer. While novel approaches like Chimeric Antigen Receptor (CAR) T cells, bispecific T cell engagers, and immune checkpoint inhibitors have shown promising efficacy, Cytokine Release Syndrome (CRS) is a serious adverse effect and remains a major concern. CRS is a phenomenon of immune hyperactivation that results in excessive cytokine secretion, and if left unchecked, it may lead to multi-organ failure and death. Here we review the pathophysiology of CRS, its occurrence and management in the context of cancer immunotherapy, and the screening approaches that can be used to assess CRS and de-risk drug discovery earlier in the clinical setting with more predictive pre-clinical data. Furthermore, the review also sheds light on the potential immunotherapeutic approaches that can be used to overcome CRS associated with T cell activation.

摘要

癌症是全球主要的死亡原因。癌症免疫疗法涉及重新激活患者自身的免疫系统来对抗癌症。虽然嵌合抗原受体 (CAR) T 细胞、双特异性 T 细胞衔接器和免疫检查点抑制剂等新方法显示出有希望的疗效,但细胞因子释放综合征 (CRS) 是一种严重的不良反应,仍然是一个主要关注点。CRS 是一种免疫过度激活的现象,导致细胞因子过度分泌,如果不加控制,可能导致多器官衰竭和死亡。在这里,我们回顾了 CRS 的病理生理学、癌症免疫疗法背景下的发生和管理,以及可用于评估 CRS 的筛选方法,并在临床环境中更早地利用更具预测性的临床前数据降低药物发现风险。此外,该综述还揭示了可用于克服与 T 细胞激活相关的 CRS 的潜在免疫治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/545e/10248525/c6f2f596e0c7/fimmu-14-1190379-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/545e/10248525/5044184808e2/fimmu-14-1190379-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/545e/10248525/824a6152b01a/fimmu-14-1190379-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/545e/10248525/73b83ff584d4/fimmu-14-1190379-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/545e/10248525/93f4f0d60147/fimmu-14-1190379-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/545e/10248525/c6f2f596e0c7/fimmu-14-1190379-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/545e/10248525/5044184808e2/fimmu-14-1190379-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/545e/10248525/824a6152b01a/fimmu-14-1190379-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/545e/10248525/73b83ff584d4/fimmu-14-1190379-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/545e/10248525/93f4f0d60147/fimmu-14-1190379-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/545e/10248525/c6f2f596e0c7/fimmu-14-1190379-g005.jpg

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Cytokine release syndrome and cancer immunotherapies - historical challenges and promising futures.

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[4]
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[5]
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[6]
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[7]
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[8]
Cytokine release syndrome and CAR T Cell therapy: Modulating the intensity of the inflammatory response and resolution within the tumor microenvironment.

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[9]
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[10]
Tumor-derived exosomes as promising tools for cancer diagnosis and therapy.

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本文引用的文献

[1]
A Probody T Cell-Engaging Bispecific Antibody Targeting EGFR and CD3 Inhibits Colon Cancer Growth with Limited Toxicity.

Cancer Res. 2022-11-15

[2]
Stage 4 Cytokine Release Syndrome Caused by the First Dose of Nivolumab and Ipilimumab Combination Therapy in a Patient with Metastatic Melanoma Successfully Treated with Methylprednisolone, Tocilizumab, and Etanercept.

Case Rep Oncol. 2022-6-27

[3]
Alternative CAR Therapies: Recent Approaches in Engineering Chimeric Antigen Receptor Immune Cells to Combat Cancer.

Biomedicines. 2022-6-24

[4]
Transcriptomic datasets of cancer patients treated with immune-checkpoint inhibitors: a systematic review.

J Transl Med. 2022-5-31

[5]
Potential Pathophysiological Mechanisms Underlying Multiple Organ Dysfunction in Cytokine Release Syndrome.

Mediators Inflamm. 2022

[6]
Chimeric antigen receptors containing the OX40 signalling domain enhance the persistence of T cells even under repeated stimulation with multiple myeloma target cells.

J Hematol Oncol. 2022-4-1

[7]
Cytokine Release Syndrome Following Blinatumomab Therapy.

Cureus. 2022-1-25

[8]
Dissecting the mechanism of cytokine release induced by T-cell engagers highlights the contribution of neutrophils.

Oncoimmunology. 2022

[9]
Trispecific T-cell engagers for dual tumor-targeting of colorectal cancer.

Oncoimmunology. 2022

[10]
Cytokine Release Syndrome in Cancer Patients Receiving Immune Checkpoint Inhibitors: A Case Series of 25 Patients and Review of the Literature.

Front Immunol. 2022

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